Lettuce variety 45-100 rz

ABSTRACT

The present invention relates to a Lactuca sativa seed designated 45-100 RZ. The present invention also relates to a Lactuca sativa plant produced by growing the 45-100 RZ seed. The invention further relates to methods for producing the lettuce cultivar, represented by lettuce variety 45-100 RZ.

INCORPORATION BY REFERENCE

This application claims priority to U.S. provisional patent applicationSer. No. 65/576,171 filed 24 Oct. 2017.

The foregoing applications, and all documents cited therein or duringtheir prosecution (“appln cited documents”) and all documents cited orreferenced in the appln cited documents, and all documents cited orreferenced herein (“herein cited documents”), and all documents cited orreferenced in herein cited documents, together with any manufacturer'sinstructions, descriptions, product specifications, and product sheetsfor any products mentioned herein or in any document incorporated byreference herein, are hereby incorporated herein by reference, and maybe employed in the practice of the invention. More specifically, allreferenced documents are incorporated by reference to the same extent asif each individual document was specifically and individually indicatedto be incorporated by reference.

FIELD OF THE INVENTION

The present invention relates to a new lettuce (Lactuca sativa) varietydesignated 45-100 RZ. Lettuce variety 45-100 RZ exhibits a combinationof traits including resistance to lettuce aphid (Nasonovia ribisnign)biotype Nr:0, resistance to root aphid (Pemphigus bursarius), resistanceto downy mildew (Bremia lactucae) races B1:1-33EU and Ca-I-VIII, maturemedium to grey green leaves with slight to no blistering and a mediumsize head.

BACKGROUND OF THE INVENTION

All cultivated forms of lettuce belong to the highly polymorphicspecies, Lactuca sativa, which is grown for its edible head and leaves.As a crop, lettuces are grown commercially wherever environmentalconditions permit the production of an economically viable yield.

Lactuca sativa is in the Cichoreae tribe of the Asteraceae (Compositae)family. Lettuce is related to chicory, sunflower, aster, scorzonera,dandelion, artichoke and chrysanthemum. Sativa is one of about 300species in the genus Lactuca.

Lettuce cultivars are susceptible to a number of pests and diseases suchas downy mildew (Bremia lactucae). Every year this disease leads tomillions of dollars of lost lettuce crop throughout the world. Downymildew (Bremia lactucae) is highly destructive on lettuce grown atrelatively low temperature and high humidity. Downy mildew is caused bya fungus, Bremia lactucae, which can be one of the following strains:NL1, NL2, NL4, NL5, NL6, NL7, NL10, NL12, NL13, NL14, NL15, NL16, B1:17,B1:18, B1:20, B1:21, B1:22, B1:23, B1:24, B1:25, B1:26, B1:27, B1:28,B1:29, B1:30, B1:31, B1:32, B1:33EU (Van Ettekoven, K. et al.,“Identification and denomination of ‘new’ races of Bremia lactucae,” In:Lebeda, A. and Kristkova, E (eds.), Eucarpia Leafy Vegetables, 1999,Palacky University, Olomouc, Czech Republic, pp. 171-175; Van der Arendet al. “Identification and denomination of “new” races of Bremialactucae in Europe by IBEB until 2002.” In: Van Hintum, Th et al.(eds.), Eucarpia Leafy Vegetables Conference 2003, Centre for GeneticResources, Wageningen, The Netherlands, p. 151; Plantum NL (Dutchassociation for breeding, tissue culture, production and trade of seedsand young plants), Van der Arend et al. “Identification and denominationof “new” races of Bremia lactucae in Europe by IBEB until 2002.” In: VanHintum, Th et al. (eds.), Eucarpia Leafy Vegetables Conference 2003,Centre for Genetic Resources, Wageningen, The Netherlands, p. 151;Plantum NL (Dutch association for breeding, tissue culture, productionand trade of seeds and young plants); IBEB press release “New race ofBremia lactucae B1:27 identified and nominated”, May 2010; Plantum NL(Dutch association for breeding, tissue culture, production and trade ofseeds and young plants), “New race of Bremia lactucae B1:28 identifiedand nominated”, March 2011; Plantum NL (Dutch association for breeding,tissue culture, production and trade of seeds and young plants), IBEBpress release, “New races of Bremia lactucae, B1:29, B1:30 and B1:31identified and nominated”, August 2013; Plantum NL (Dutch associationfor breeding, tissue culture, production and trade of seeds and youngplants), IBEB press release, “A new race of Bremia lactucae, B1:32identified and nominated in Europe”, May 2015), Plantum NL (Dutchassociation for breeding, tissue culture, production and trade of seedsand young plants), IBEB-EU press release, “A new race of Bremialactucae, B1:33EU identified and denominated in Europe”, May 2017, Ca-I,Ca-IIA, Ca-IIB, Ca-III, Ca-IV (Schettini, T. M., Legg, E. J.,Michelmore, R. W., 1991). Insensitivity to metalaxyl in Californiapopulations of Bremia lactucae and resistance of California lettucecultivars to downy mildew. Phytopathology 81(1). p. 64-70), and Ca-V,Ca-VI, Ca-VII, Ca-VIII (Michelmore R. & Ochoa. 0. “Breeding CrispheadLettuce. “In: California Lettuce Research Board, Annual Report2005-2006, 2006, Salinas, Calif., pp. 55-68).

Downy mildew causes pale, angular, yellow areas bounded by veins on theupper leaf surfaces. Sporulation occurs on the opposite surface of theleaves. The lesions eventually turn brown, and they may enlarge andcoalesce. These symptoms typically occur first on the lower leaves ofthe lettuce, but under ideal conditions may move into the upper leavesof the head. When the fungus progresses to this degree, the head cannotbe harvested. Less severe damage requires the removal of more leavesthan usual, especially when the lettuce reaches its final destination.

Of the various species of aphids that feed on lettuce, thecurrant-lettuce aphid (Nasonovia ribisnigri) is the most destructivespecies because it feeds both on the leaves of the lettuce as well asthe heart of the lettuce, making it difficult to control withconventional insecticides. The lettuce aphid feeds by sucking sap fromthe lettuce leaves. Although direct damage to the lettuce may belimited, its infestation has serious consequences because the presenceof aphids makes lettuce unacceptable to consumers.

Lettuce root aphids (Pemphigus bursarius) form clustered colonies onlettuce roots, covering them with a white powdery wax. Feeding on theroots cause the plants to wilt during the day. Individually affectedrootlets turn brown and die. The developing heads remain soft, may failto develop, and yields thus become reduced. Prolonged periods ofinfestation can cause the collapse and death of the plant.

The head size of iceberg lettuce is a measure of yield. This isespecially true in the production of iceberg lettuce heads to be used inprocessing, where yield is a very important trait. An iceberg lettucevariety used in processing should have at least a medium head size.

The outer leaves, although not harvested, are considered important byiceberg lettuce growers because of their photosynthesis potential, andtheir ability to protect the final product, the iceberg head, fromenvironmental damage such as extreme sunshine exposure, frost, or hail,and other potentially damaging external factors. The protective andproduction potential of large outer leaves are thus preferred over smallouter leaves. Vegetables are generally considered healthy foods. Bothconsumers as well as producers benefit from an increase of vegetableconsumption. Higher vegetable consumption can be promoted by education,marketing, and improvement of certain product traits, such as taste,aroma, and visual attractiveness. Visual attractiveness of iceberglettuce heads is promoted by the absence of leaf damage and relateddiscolorations, and a fresh, shiny green color. Amongst icebergvarieties there exists genetic variability in the glossiness of the headleaves.

Citation or identification of any document in this application is not anadmission that such document is available as prior art to the presentinvention.

SUMMARY OF THE INVENTION

Given the need expressed by relevant stakeholders for a lettuce varietywhich exhibits a combination of traits including resistance to lettuceaphid Nasonovia ribisnigri (Mosley) biotype Nr:0, resistance to rootaphid (Pemphigus bursarius), resistance to downy mildew (Bremialactucae) races B1:1-33EU and Ca-I-VIII, mature medium to grey greenleaves with slight to no blistering and a medium size head, the presentinvention addresses this need by providing a new type of lettuce(Lactuca sativa) variety, designated 45-100 RZ.

The present invention provides a new lettuce (Lactuca sativa) varietydesignated 45-100 RZ. This new lettuce variety exhibits a combination oftraits including resistance to lettuce aphid Nasonovia ribisnigri(Mosley) biotype Nr:0, resistance to root aphid (Pemphigus bursarius),resistance to downy mildew (Bremia lactucae) races B1:1-33EU andCa-I-VIII, mature medium to grey green leaves with slight to noblistering and a medium size head.

The present invention provides seed of a lettuce (Lactuca sativa)variety designated 45-100 RZ. A sample of seeds of said lettuce variety,have been deposited with the National Collections of Industrial, Marineand Food Bacteria (NCIMB) in Bucksburn, Aberdeen AB21 9YA, Scotland, UKand have been assigned NCIMB Accession No. NCIMB 42847.

In one embodiment, the invention provides a lettuce plant grown from theseed of lettuce (Lactuca sativa) variety 45-100 RZ.

In another embodiment, the invention provides a lettuce plant designated45-100 RZ, which is a plant grown from seed having been deposited underNCIMB Accession No. NCIMB 42847.

In one embodiment, the invention provides for a lettuce plant which maycomprise genetic information for exhibiting all of the physiological andmorphological characteristics of a plant of the invention, wherein thegenetic information is as contained in a plant, a sample of seed of saidvariety having been deposited under NCIMB Accession No. NCIMB 42847.

In one embodiment, the invention provides for a lettuce plant exhibitingall the physiological and morphological characteristics of a plant ofthe invention, and having the genetic information for so exhibiting thecombination of traits, wherein the genetic information is as containedin a plant, a sample of seed of said variety having been deposited underNCIMB Accession No. NCIMB 42847.

In an embodiment of the present invention, there also is provided partsof a lettuce plant of the invention, which may include parts of alettuce plant exhibiting all the physiological and morphologicalcharacteristics of a plant of the invention, or parts of a lettuce planthaving any of the mentioned resistance(s) and a combination of traitsincluding one or more or all morphological and physiologicalcharacteristics tabulated herein, including parts of lettuce variety45-100 RZ, wherein the plant parts are involved in sexual reproduction,which include, without limitation, microspores, pollen, ovaries, ovules,embryo sacs or egg cells and/or wherein the plant parts are suitable forvegetative reproduction, which include, without limitation, cuttings,roots, stems, cells or protoplasts and/or wherein the plant parts aretissue culture of regenerable cells in which the cells or protoplasts ofthe tissue culture are derived from a tissue such as, for example andwithout limitation, leaves, pollen, embryos, cotyledon, hypocotyls,meristematic cells, roots, root tips, anthers, flowers, seeds or stems.The plants of the invention from which such parts may come from includethose wherein a sample of seed of which having been deposited underNCIMB Accession No. NCIMB 42847 or lettuce variety or cultivardesignated 45-100 RZ, as well as seed from such a plant, plant parts ofsuch a plant (such as those mentioned herein) and plants from such seedand/or progeny of such a plant, advantageously progeny exhibiting suchcombination of such traits, each of which, is within the scope of theinvention; and such combination of traits.

In a further embodiment there is a plant regenerated from theabove-described plant parts or regenerated from the above-describedtissue culture. Advantageously such a plant may have morphologicaland/or physiological characteristics of lettuce variety 45-100 RZ and/orof a plant grown from seed, a sample of seed of which having beendeposited under NCIMB Accession No. NCIMB 42847—including withoutlimitation such plants having all of the physiological and morphologicalcharacteristics of lettuce variety 45-100 RZ and/or of a plant grownfrom seed, a sample of seed of which having been deposited under NCIMBAccession No. NCIMB 42847.

Accordingly, in still a further embodiment, there is provided a lettuceplant having all of the physiological and morphological characteristicsof lettuce variety 45-100 RZ, a sample of seed of which having beendeposited under NCIMB Accession No. 42847. Such a plant may be grownfrom the seeds, regenerated from the above-described plant parts, orregenerated from the above-described tissue culture. A lettuce planthaving any of the aforementioned resistance(s), and one or moremorphological or physiological characteristics recited or tabulatedherein, and a lettuce plant advantageously having all of theaforementioned resistances and the characteristics recited and tabulatedherein, are preferred. Parts of such plants—such as those plant partsabove-mentioned—are encompassed by the invention.

In a further aspect, the invention provides a method of vegetativelypropagating a plant of lettuce variety 45-100 RZ which may comprise (a)collecting tissue capable of being propagated from a plant of lettuce45-100 RZ, a sample of seed of said variety having been deposited underNCIMB accession No. 42847 and (b) cultivating the tissue to obtainproliferated shoots and rooting the proliferated shoots to obtain rootedplantlets. Optionally the invention further may comprise growing plantsfrom the rooted plantlets. Plantlets and plants produced by thesemethods, are encompassed by the invention.

In one embodiment, there is provided a method for producing a progeny oflettuce cultivar 45-100 RZ which may comprise crossing a plantdesignated 45-100 RZ with itself or with another lettuce plant,harvesting the resultant seed, and growing said seed.

In a further embodiment, a progeny plant is provided which is producedby this method, wherein said progeny exhibits a combination of traitsincluding resistance to lettuce aphid Nasonovia ribisnigri (Mosley)biotype Nr:0, resistance to root aphid, resistance to downy mildew(Bremia lactucae) races B1:1-33EU and Ca-I-VIII, mature medium to greygreen leaves with slight to no blistering and a medium size head.

In another embodiment, a progeny plant is provided which is produced bythe above method, wherein said progeny exhibits all the morphologicaland physiological characteristics of the lettuce variety designated45-100 RZ, a sample of seed of said variety having been deposited underNCIMB accession No. 42847.

In a further embodiment there is provided a progeny plant produced bysexual or vegetative reproduction, grown from seeds, regenerated fromthe above-described plant parts, or regenerated from the above-describedtissue culture of the lettuce cultivar or a progeny plant thereof, asample of seed of which having been deposited under NCIMB Accession No.42847. The progeny may have any of the aforementioned resistance(s), andone or more morphological or physiological characteristics recited ortabulated herein, and a progeny plant advantageously having all of theaforementioned resistances and the characteristics recited and tabulatedherein, are preferred.

Progeny of the lettuce variety 45-100 RZ may be modified in one or moreother characteristics, in which the modification is a result of, forexample and without limitation, mutagenesis or transformation with atransgene.

In still another embodiment, the present invention provides progeny oflettuce cultivar 45-100 RZ produced by sexual or vegetativereproduction, grown from seed, regenerated from the above-describedplant parts, or regenerated from the above-described tissue culture ofthe lettuce cultivar or a progeny plant thereof.

In still a further embodiment, the invention provides a method ofproducing a lettuce seed which may comprise crossing a male parentlettuce plant with a female parent lettuce plant and harvesting theresultant lettuce seed, in which the male parent lettuce plant or thefemale parent lettuce plant is a lettuce plant of the invention, e.g. alettuce plant having all of the morphological or physiologicalcharacteristics tabulated herein, including a lettuce plant of lettucecultivar 45-100 RZ, a sample of seed of which having been depositedunder NCIMB 42847. The resultant lettuce seed produced by this methodand the lettuce plant that is produced by growing said lettuce seed alsoforms part of the invention.

In still a further embodiment, the invention provides a method ofproducing a lettuce cultivar which exhibits all of the physiological andmorphological characteristics of lettuce variety 45-100 RZ, a sample ofseed of said variety having been deposited under NCIMB accession No.42847.

The invention further relates to a method for producing a seed of a45-100 RZ-derived lettuce plant which may comprise (a) crossing a plantof lettuce variety 45-100 RZ, a sample of seed of which having beendeposited under NCIMB Accession No. NCIMB 42847, with a second lettuceplant, and (b) whereby seed of a 45-100 RZ-derived lettuce plant form.This method may further comprise (c) crossing a plant grown from 45-100RZ-derived lettuce seed with itself or with a second lettuce plant toyield additional 45-100 RZ-derived lettuce seed, (d) growing theadditional 45-100 RZ-derived lettuce seed of step (c) to yieldadditional 45-100 RZ-derived lettuce plants, and (e) repeating thecrossing and growing of steps (c) and (d) for an additional 3-10generations to generate further 45-100 RZ-derived lettuce plants, and(f) whereby seed of a 45-100 RZ-derived lettuce plant form. A seedproduced by this method and a plant grown from said seed also form partof the invention.

The invention also relates to a method of introducing at least one newtrait into a plant of lettuce variety 45-100 RZ which may comprise: (a)crossing a plant of lettuce variety 45-100 RZ, a sample of seed of whichhaving been deposited under NCIMB Accession No. NCIMB 42847, with asecond lettuce plant that may comprise at least one new trait to produceprogeny seed, (b) harvesting and planting the progeny seed to produce atleast one progeny plant of a subsequent generation, wherein the progenyplant may comprise the at least one new trait, (c) crossing the progenyplant with a plant of lettuce variety 45-100 RZ to produce backcrossprogeny seed, (d) harvesting and planting the backcross progeny seed toproduce a backcross progeny plant, and (e) repeating steps (c) and (d)for at least three additional generations to produce a lettuce plant ofvariety 45-100 RZ which may comprise at least one new trait and all ofthe physiological and morphological characteristics of a plant oflettuce variety 45-100 RZ, when grown in the same environmentalconditions. A lettuce plant produced by this method also forms part ofthe invention.

The invention further relates to a method of producing a plant oflettuce variety 45-100 RZ which may comprise at least one new trait, themethod which may comprise introducing a mutation or transgene conferringthe at least one new trait into a plant of lettuce variety 45-100 RZ,wherein a sample of seed of said variety has been deposited under NCIMBAccession No. NCIMB 42847. A lettuce plant produce by this method alsoforms part of the invention.

The invention even further relates to a method of producing lettuceleaves as a food product which may comprise: (a) sowing a seed oflettuce variety 45-100 RZ, a sample of seed of which having beendeposited under NCIMB Accession No. NCIMB 42847, (b) growing said seedinto a harvestable lettuce plant and (c) harvesting lettuce leaves orheads from the plant. The invention further comprehends packaging and/orprocessing the lettuce plants, heads or leaves.

Also encompassed by the invention is a container which may comprise oneor more lettuce plants of the invention for harvest of leaves.

Further encompassed by the invention is a method of determining thegenotype of a plant of lettuce variety 45-100 RZ, a sample of seed ofwhich has been deposited under NCIMB Accession No. NCIMB 42847, or afirst generation progeny thereof, which may comprise obtaining a sampleof nucleic acids from said plant and comparing said nucleic acids to asample of nucleic acids obtained from a reference plant, and detecting aplurality of polymorphisms between the two nucleic acid samples, whereinthe plurality of polymorphisms are indicative of lettuce variety 45-100RZ and/or give rise to the expression of any one or more, or all, of thephysiological and morphological characteristics of lettuce variety45-100 RZ of the invention.

Accordingly, it is an object of the invention to not encompass withinthe invention any previously known product, process of making theproduct, or method of using the product such that Applicants reserve theright and hereby disclose a disclaimer of any previously known product,process, or method. It is further noted that the invention does notintend to encompass within the scope of the invention any product,process, or making of the product or method of using the product, whichdoes not meet the written description and enablement requirements of theUSPTO (35 U.S.C. § 112, first paragraph), such that Applicants reservethe right and hereby disclose a disclaimer of any previously describedproduct, process of making the product, or method of using the product.

It is noted that in this disclosure and particularly in the claims,terms such as “comprises”, “comprised”, and “comprising” and the like(e.g., “includes”, “included”, “including”, “contains”, “contained”,“containing”, “has”, “had”, “having”, etc.) can have the meaningascribed to them in US patent law, i.e., they are open ended terms. Forexample, any method that “comprises,” “has” or “includes” one or moresteps is not limited to possessing only those one or more steps and alsocovers other unlisted steps. Similarly, any plant that “comprises,”“has” or “includes” one or more traits is not limited to possessing onlythose one or more traits and covers other unlisted traits. Similarly,the terms “consists essentially of” and “consisting essentially of” havethe meaning ascribed to them in US patent law, e.g., they allow forelements not explicitly recited, but exclude elements that are found inthe prior art or that affect a basic or novel characteristic of theinvention. See also MPEP § 2111.03. In addition, the term “about” isused to indicate that a value includes the standard deviation of errorfor the device or method being employed to determine the value.

These and other embodiments are disclosed or are obvious from andencompassed by the following Detailed Description.

DEPOSIT

The Deposit with NCIMB Ltd, Ferguson Building, Craibstone Estate,Bucksburn, Aberdeen AB21 9YA, UK, on Oct. 20, 2017, under depositaccession number NCIMB 42847 was made pursuant to the terms of theBudapest Treaty. Upon issuance of a patent, all restrictions upon thedeposit will be removed, and the deposit is intended to meet therequirements of 37 CFR §§ 1.801-1.809. The deposit will be irrevocablyand without restriction or condition released to the public upon theissuance of a patent and for the enforceable life of the patent. Thedeposit will be maintained in the depository for a period of 30 years,or 5 years after the last request, or for the effective life of thepatent, whichever is longer, and will be replaced if necessary duringthat period.

BRIEF DESCRIPTION OF THE DRAWINGS

The patent or application file contains at least one drawing executed incolor. Copies of this patent or patent application publication withcolor drawing(s) will be provided by the Office upon request and paymentof the necessary fee.

The following detailed description, given by way of example, but notintended to limit the invention solely to the specific embodimentsdescribed, may best be understood in conjunction with the accompanyingdrawing, in which:

FIG. 1 is an illustration of six different shapes of the fourth leaffrom a 20-day old seedling grown under optimal conditions.

FIG. 2 is a picture of the shape of the fourth leaf of 45-100 RZ.

FIG. 3 is a picture of the shape of a mature leaf of 45-100 RZ.

DETAILED DESCRIPTION OF THE INVENTION

The invention provides methods and compositions relating to plants,seeds and derivatives of a new lettuce variety herein referred to aslettuce variety 45-100 RZ. Lettuce variety 45-100 RZ is a uniform andstable line, distinct from other such lines.

In a preferred embodiment, the specific type of breeding method employedfor developing a lettuce cultivar is pedigree selection, where bothsingle plant selection and mass selection practices are employed.Pedigree selection, also known as the “Vilmorin system of selection,” isdescribed in Fehr, W., Principles of Cultivar Development, Volume I,MacMillan Publishing Co., which is hereby incorporated by reference.

When pedigree selection is applied, in general selection is firstpracticed among F₂ plants. In the next season, the most desirable F₃lines are first identified, and then desirable F₃ plants within eachline are selected. The following season and in all subsequentgenerations of inbreeding, the most desirable families are identifiedfirst, then desirable lines within the selected families are chosen, andfinally desirable plants within selected lines are harvestedindividually. A family refers to lines that were derived from plantsselected from the same progeny from the preceding generation.

Using this pedigree method, two parents may be crossed using anemasculated female and a pollen donor (male) to produce F₁ offspring.Lettuce is an obligate self-pollination species, which means that pollenis shed before stigma emergence, assuring 100% self-fertilization.Therefore, in order to optimize crossing, a method of misting may beused to wash the pollen off prior to fertilization to assure crossing orhybridization.

Parental varieties are selected from commercial varieties thatindividually exhibit one or more desired phenotypes. Additionally, anybreeding method involving selection of plants for the desired phenotypemay be used in the method of the present invention.

The F₁ may be self-pollinated to produce a segregating F₂ generation.Individual plants may then be selected which represent the desiredphenotype in each generation (F₃, F₄, F₅, etc.) until the traits arehomozygous or fixed within a breeding population.

A detailed description of the development of lettuce variety 45-100 RZis described in Table 1. The seedlot in year 6, seedlot 15R.5058, wasdeposited with the NCIMB under deposit number NCIMB 42847.

TABLE 1 Year Description Location 0 Final F1-cross plant 08V.50693 ×Fijnaart, The Netherlands plant 08V.50587 in glasshouse. 0-1 F1 plantgrown for F2 seed Fijnaart, The Netherlands production in glasshouse. 1F2 plant selected in open field, Fijnaart, The Netherlands followed byF3 seed. 2 F3 plant selected in open field, Murcia, Spain followed by F4seed. 3 F4 plant selected in open field, Fijnaart, The Netherlands TheNetherlands, followed by F5 seed. 4-5 F5 plant selected in open field,Murcia, Spain followed by F6 seed. 5 F6 plant selected in open field,Fijnaart, the Netherlands followed by F7 seed. 6 F7 populationestablished uniform, Daylesford, Australia multiplied in plastic tunnel,seed lot 15R.5058.

In one embodiment, a plant of the invention has all the physiologicaland morphological characteristics of lettuce variety 45-100 RZ. Thesecharacteristics of a lettuce plant of the invention, e.g. variety 45-100RZ, are summarized in Tables 2 and 3.

Next to the physiological and morphological characteristics mentioned inTables 2 and 3, a plant of the invention also exhibits resistance todowny mildew (Bremia lactucae Regel.) races.

As used herein resistance against Bremia lactucae is defined as theability of a plant to resist infection by each of the various strainsB1:1 to B1:33EU, Ca-I to Ca-VIII of Bremia lactucae Regel. in all stagesbetween the seedling stage and the harvestable plant stage. B1:1 toB1:33EU means strains NL1, NL2, NL4, NL5, NL6, NL7, NL10, NL12, NL13,NL14, NL15, NL16, B1:17, B1:18, B1:20, B1:21, B1:22, B1:23, B1:24,B1:25, B1:26, B1:27, B1:28, B1:29, B1:30, B1:31, B1:32, B1:33EU (VanEttekoven K, Van der Arend A J M, 1999. identification and denominationof ‘new’ races of Bremia lactucae. In: Lebeda A, Kristkova E (eds.)Eucarpia leafy vegetables '99. Palacky University, Olomouc, CzechRepublic, 1999: 171-175; Van der Arend, A. J. M., Gautier, J., Guenard,M., Michel, H., Moreau, B., de Ruijter, J., Schut, J. W. and de Witte,I. (2003). Identification and denomination of ‘new’ races of Bremialactucae in Europe by IBEB until 2002. In: Eucarpia leafy vegetables2003. Proceedings of the Eucarpia Meeting on leafy vegetables geneticsand breeding. Noorwijkerhout, The Netherlands. Eds. Van Hintum T.,Lebeda A., Pink D., Schut J. pp 151-160; Van der Arend A J M, Gautier J,Grimault V, Kraan P, Van der Laan R, Mazet J, Michel H, Schut J W,Smilde D, De Witte I (2006) Identification and denomination of “new”races of Bremia lactucae in Europe by IBEB until 2006; incorporatedherein by reference; Plantum NL (Dutch association for breeding, tissueculture, production and trade of seeds and young plants), IBEB pressrelease, “New race of Bremia lactucae B1:27 identified and nominated”,May 2010; Plantum NL (Dutch association for breeding, tissue culture,production and trade of seeds and young plants), IBEB press release,“New race of Bremia lactucae B1:28 identified and nominated”, March2011; Plantum NL (Dutch association for breeding, tissue culture,production and trade of seeds and young plants), IBEB press release,“New races of Bremia lactucae, B1:29, B1:30 and B1:31 identified andnominated”, August 2013; Plantum NL (Dutch association for breeding,tissue culture, production and trade of seeds and young plants), IBEBpress release, “A new race of Bremia lactucae, B1:32 identified andnominated in Europe”, May 2015; Plantum NL (Dutch association forbreeding, tissue culture, production and trade of seeds and youngplants), IBEB-EU press release, “A new race of Bremia lactucae, B1:33 EUidentified and denominated in Europe”, May 2017. Ca-I to Ca-VIII meansCa-I, Ca-IIA, Ca-IIB, Ca-III, Ca-IV (Schettini, T. M., Legg, E. J.,Michelmore, R. W., 1991). Insensitivity to metalaxyl in Californiapopulations of Bremia lactucae and resistance of California lettucecultivars to downy mildew, Phytopathology 81(1). p. 64-′70), and Ca-V,Ca-VI, Ca-VII, Ca-VIII (Michelmore R. & Ochoa. O., “Breeding CrispheadLettuce, “In: California Lettuce Research Board, Annual Report2005-2006, 2006, Salinas, Calif., pp. 55-68).

Resistance typically is tested by two interchangeable methods, describedby Bonnier, F. J. M. et al. (Euphytica, 61(3):203-211, 1992;incorporated herein by reference). One method involves inoculating 7-dayold seedlings, and observing sporulation 10 to 14 days later. The othermethod involves inoculating leaf discs with a diameter of 18 mm obtainedfrom a non-senescent, fully grown true leaf and observing sporulation 10days later.

As used herein, resistance against Nasonovia ribisnigri (Mosley), orcurrant-lettuce aphid, is defined as the plant characteristic whichresults in a non-feeding response of the aphid on the leaves of theplant in all stages between 5 true-leaf stage and harvestable plantstage (U.S. Pat. No. 5,977,443 to Jansen, J. P. A., “Aphid Resistance inComposites,” p. 12, 1999; incorporated herein by reference).

Resistance is tested by spreading at least ten aphids of biotype Nr:0 ona plant in a plant stage between 5 true leaves and harvestable stage,and observing the density of the aphid population on the plant as wellas the growth reduction after 14 days in a greenhouse, with temperaturesettings of 23 degrees Celsius in daytime and 21 degrees Celsius atnight. Day length is kept at 18 hours by assimilation lights.

As used herein, resistance to Pemphigus bursarius, or root aphid, isdefined as the ability of a plant to resist infection to root aphids.Resistance may be tested by the method described by Ellis et al., (1994,Annals of Applied Biology 124:141-151; incorporated herein byreference).

As used herein, the color of the mature leaves is defined by the colorof a fully-grown tenth to fifteenth leaf, which should be similar to ordarker than RHS N77 (The Royal Horticultural Society, London, UK).

Embodiments of the inventions advantageously have one or more, and mostadvantageously all, of these characteristics.

In Table 2, the seed color, cotyledon shape and characteristics of thefourth leaf of “45-100 RZ” are shown.

TABLE 2 Character “45-100 RZ” Plant Type Salinas Seed Color Black (GreyBrown) Cotyledon Shape Intermediate Shape of Fourth Leaf ElongatedRolling of Fourth Leaf Apical margin Cupping of Fourth Leaf SlightFourth Leaf Apical Margin Incised Fourth Leaf Basal Margin IncisedUndulation Slight Green color Medium Green Anthocyanin distributionAbsent

In Table 3, the mature leaf and head characteristics of “45-100 RZ” areshown.

TABLE 3 Character “45-100 RZ” Leaf Color Medium Green AnthocyaninDistribution Absent Margin Incision Depth Absent/Shallow to ModerateMargin Indentation Shallowly Dentate Undulations of the Apical MarginModerate Leaf Size Medium Leaf Glossiness Dull Leaf BlisteringAbsent/Slight Leaf Thickness Thick Trichomes Absent Head Shape SphericalButt Shape Rounded Midrib Prominently Raised

In one aspect the invention provides a new type of lettuce (Lactucasativa) variety, designated 45-100 RZ. Lettuce cultivar 45-100 RZexhibits a combination of traits including resistance to lettuce aphidNasonovia ribisnigri (Mosley) biotype Nr:0, resistance to root aphid(Pemphigus bursarius), resistance to downy mildew (Bremia lactucae)races B1:1-33EU and Ca-I-VIII, mature medium to grey green leaves withslight to no blistering and a medium size head.

In an embodiment, the invention relates to lettuce plants that have allthe physiological and morphological characteristics of the invention andhave acquired said characteristics by introduction of the geneticinformation that is responsible for the characteristics from a suitablesource, either by conventional breeding, or genetic modification, inparticular by cisgenesis or transgenesis. Cisgenesis is geneticmodification of plants with a natural gene, coding for an (agricultural)trait, from the crop plant itself or from a sexually compatible donorplant. Transgenesis is genetic modification of a plant with a gene froma non-crossable species or a synthetic gene.

Just as useful traits that may be introduced by backcrossing, usefultraits may be introduced directly into the plant of the invention, beinga plant of lettuce variety 45-100 RZ, by genetic transformationtechniques; and, such plants of lettuce variety 45-100 RZ that haveadditional genetic information introduced into the genome or thatexpress additional traits by having the DNA coding there for introducedinto the genome via transformation techniques, are within the ambit ofthe invention, as well as uses of such plants, and the making of suchplants.

Genetic transformation may therefore be used to insert a selectedtransgene into the plant of the invention, being a plant of lettucevariety 45-100 RZ or may, alternatively, be used for the preparation oftransgenes which may be introduced by backcrossing. Methods for thetransformation of plants, including lettuce, are well known to those ofskill in the art.

Vectors used for the transformation of lettuce cells are not limited solong as the vector may express an inserted DNA in the cells. Forexample, vectors, which may comprise promoters for constitutive geneexpression in lettuce cells (e.g., cauliflower mosaic virus 35Spromoter) and promoters inducible by exogenous stimuli, may be used.Examples of suitable vectors include pBI binary vector. The “lettucecell” into which the vector is to be introduced includes various formsof lettuce cells, such as cultured cell suspensions, protoplasts, leafsections, and callus. A vector may be introduced into lettuce cells byknown methods, such as the polyethylene glycol method, polycationmethod, electroporation, Agrobacterium-mediated transfer, particlebombardment and direct DNA uptake by protoplasts. To effecttransformation by electroporation, one may employ either friabletissues, such as a suspension culture of cells or embryogenic callus oralternatively one may transform immature embryos or other organizedtissue directly. In this technique, one would partially degrade the cellwalls of the chosen cells by exposing them to pectin-degrading enzymes(pectolyases) or mechanically wound tissues in a controlled manner.

A particularly efficient method for delivering transforming DNA segmentsto plant cells is microprojectile bombardment. In this method, particlesare coated with nucleic acids and delivered into cells by a propellingforce. Exemplary particles include those which may be comprised oftungsten, platinum, and preferably, gold. For the bombardment, cells insuspension are concentrated on filters or solid culture medium.Alternatively, immature embryos or other target cells may be arranged onsolid culture medium. The cells to be bombarded are positioned at anappropriate distance below the macroprojectile stopping plate. Anillustrative embodiment of a method for delivering DNA into plant cellsby acceleration is the Biolistics Particle Delivery System, which may beused to propel particles coated with DNA or cells through a screen, suchas a stainless steel or Nytex screen, onto a surface covered with targetlettuce cells. The screen disperses the particles so that they are notdelivered to the recipient cells in large aggregates. It is believedthat a screen intervening between the projectile apparatus and the cellsto be bombarded reduces the size of projectiles aggregate and maycontribute to a higher frequency of transformation by reducing thedamage inflicted on the recipient cells by projectiles that are toolarge. Microprojectile bombardment techniques are widely applicable, andmay be used to transform virtually any plant species, including a plantof lettuce variety 45-100 RZ.

Agrobacterium-mediated transfer is another widely applicable system forintroducing gene loci into plant cells. An advantage of the technique isthat DNA may be introduced into whole plant tissues, thereby bypassingthe need for regeneration of an intact plant from a protoplast.Agrobacterium transformation vectors are capable of replication in E.coli as well as Agrobacterium, allowing for convenient manipulations.Moreover, advances in vectors for Agrobacterium-mediated gene transferhave improved the arrangement of genes and restriction sites in thevectors to facilitate the construction of vectors capable of expressingvarious polypeptide coding genes. The vectors have convenientmulti-linker regions flanked by a promoter and a polyadenylation sitefor direct expression of inserted polypeptide coding genes.Additionally, Agrobacterium containing both armed and disarmed Ti genesmay be used for transformation. In those plant strains whereAgrobacterium-mediated transformation is efficient, it is the method ofchoice because of the facile and defined nature of the gene locustransfer. The use of Agrobacterium-mediated plant integrating vectors tointroduce DNA into plant cells, including lettuce plant cells, is wellknown in the art (See, e.g., U.S. Pat. Nos. 7,250,560 and 5,563,055).

Transformation of plant protoplasts also may be achieved using methodsbased on calcium phosphate precipitation, polyethylene glycol treatment,electroporation, and combinations of these treatments.

A number of promoters have utility for plant gene expression for anygene of interest including but not limited to selectable markers,scoreable markers, genes for pest tolerance, disease resistance,nutritional enhancements and any other gene of agronomic interest.Examples of constitutive promoters useful for lettuce plant geneexpression include, but are not limited to, the cauliflower mosaic virus(CaMV) P-35S promoter, a tandemly duplicated version of the CaMV 35Spromoter, the enhanced 35S promoter (P-e35S), the nopaline synthasepromoter, the octopine synthase promoter, the figwort mosaic virus(P-FMV) promoter (see U.S. Pat. No. 5,378,619), an enhanced version ofthe FMV promoter (P-eFMV) where the promoter sequence of P-FMV isduplicated in tandem, the cauliflower mosaic virus 19S promoter, asugarcane bacilliform virus promoter, a commelina yellow mottle viruspromoter, the promoter for the thylakoid membrane proteins (psaD, psaF,psaE, PC, FNR, atpC, atpD, cab, rbcS) (see U.S. Pat. No. 7,161,061), theCAB-1 promoter (see U.S. Pat. No. 7,663,027), the promoter from maizeprolamin seed storage protein (see U.S. Pat. No. 7,119,255), and otherplant DNA virus promoters known to express in plant cells. A variety ofplant gene promoters that are regulated in response to environmental,hormonal, chemical, and/or developmental signals may be used forexpression of an operably linked gene in plant cells, includingpromoters regulated by (1) heat, (2) light (e.g., pea rbcS-3A promoter,maize rbcS promoter, or chlorophyll a/b-binding protein promoter), (3)hormones, such as abscisic acid, (4) wounding (e.g., wunl, or (5)chemicals such as methyl jasmonate, salicylic acid, or Safener. It mayalso be advantageous to employ organ-specific promoters.

Exemplary nucleic acids which may be introduced to the lettuce varietyof this invention include, for example, DNA sequences or genes fromanother species, or even genes or sequences which originate with or arepresent in lettuce species, but are incorporated into recipient cells bygenetic engineering methods rather than classical reproduction orbreeding techniques. However, the term “exogenous” is also intended torefer to genes that are not normally present in the cell beingtransformed, or perhaps simply not present in the form, structure, etc.,as found in the transforming DNA segment or gene, or genes which arenormally present and that one desires to express in a manner thatdiffers from the natural expression pattern, e.g., to over-express.Thus, the term “exogenous” gene or DNA is intended to refer to any geneor DNA segment that is introduced into a recipient cell, regardless ofwhether a similar gene may already be present in such a cell. The typeof DNA included in the exogenous DNA may include DNA which is alreadypresent in the plant cell, DNA from another plant, DNA from a differentorganism, or a DNA generated externally, such as a DNA sequencecontaining an antisense message of a gene, or a DNA sequence encoding asynthetic or modified version of a gene.

Many hundreds if not thousands of different genes are known and couldpotentially be introduced into a plant of lettuce variety 45-100 RZ.Non-limiting examples of particular genes and corresponding phenotypesone may choose to introduce into a lettuce plant include one or moregenes for insect tolerance, pest tolerance such as genes for fungaldisease control, herbicide tolerance, and genes for quality improvementssuch as yield, nutritional enhancements, environmental or stresstolerances, or any desirable changes in plant physiology, growth,development, morphology or plant product(s).

Alternatively, the DNA coding sequences may affect these phenotypes byencoding a non-translatable RNA molecule that causes the targetedinhibition of expression of an endogenous gene, for example viaantisense- or cosuppression-mediated mechanisms. The RNA could also be acatalytic RNA molecule (i.e., a ribozyme) engineered to cleave a desiredendogenous mRNA product. Thus, any gene which produces a protein or mRNAwhich expresses a phenotype or morphology change of interest is usefulfor the practice of the present invention. (See also U.S. Pat. No.7,576,262, “Modified gene-silencing RNA and uses thereof.”)

U.S. Pat. Nos. 7,230,158, 7,122,720, 7,081,363, 6,734,341, 6,503,732,6,392,121, 6,087,560, 5,981,181, 5,977,060, 5,608,146, 5,516,667, eachof which, and all documents cited therein are hereby incorporated hereinby reference, consistent with the above INCORPORATION BY REFERENCEsection, are additionally cited as examples of U.S. patents that mayconcern transformed lettuce and/or methods of transforming lettuce orlettuce plant cells, and techniques from these US patents, as well aspromoters, vectors, etc., may be employed in the practice of thisinvention to introduce exogenous nucleic acid sequence(s) into a plantof lettuce variety 45-100 RZ (or cells thereof), and exemplify someexogenous nucleic acid sequence(s) which may be introduced into a plantof lettuce variety 45-100 RZ (or cells thereof) of the invention, aswell as techniques, promoters, vectors etc., to thereby obtain furtherplants of lettuce variety 45-100 RZ, plant parts and cells, seeds, otherpropagation material harvestable parts of these plants, etc. of theinvention, e.g. tissue culture, including a cell or protoplast, such asan embryo, meristem, cotyledon, pollen, leaf, anther, root, root tip,pistil, flower, seed or stalk.

The invention further relates to propagation material for producingplants of the invention. Such propagation material may comprise interalia seeds of the claimed plant and parts of the plant that are involvedin sexual reproduction. Such parts are for example selected from thegroup consisting of seeds, microspores, pollen, ovaries, ovules, embryosacs and egg cells. In addition, the invention relates to propagationmaterial which may comprise parts of the plant that are suitable forvegetative reproduction, for example cuttings, roots, stems, cells,protoplasts.

According to a further aspect thereof the propagation material of theinvention may comprise a tissue culture of the claimed plant. The tissueculture may comprise regenerable cells. Such tissue culture may bederived from leaves, pollen, embryos, cotyledon, hypocotyls,meristematic cells, roots, root tips, anthers, flowers, seeds and stems.(See generally U.S. Pat. No. 7,041,876 on lettuce being recognized as aplant that may be regenerated from cultured cells or tissue).

Also, the invention comprehends methods for producing a seed of a“45-100 RZ”-derived lettuce plant which may comprise (a) crossing aplant of lettuce variety 45-100 RZ, a sample of seed of which havingbeen deposited under NCIMB Accession No. NCIMB 42847, with a secondlettuce plant, and (b) whereby seed of a 45-100 RZ-derived lettuce plantform. Such a method may further comprise (c) crossing a plant grown from45-100 RZ-derived lettuce seed with itself or with a second lettuceplant to yield additional 45-100 RZ-derived lettuce seed, (d) growingthe additional 45-100 RZ-derived lettuce seed of step (c) to yieldadditional 45-100 RZ-derived lettuce plants, and (e) repeating thecrossing and growing of steps (c) and (d) for an additional 3-10generations to further generate 45-100 RZ-derived lettuce plants.

The invention further relates to the above methods that may furthercomprise selecting at steps b), d), and e), a 45-100 RZ-derived lettuceplant, exhibiting one or more or all of the physiological andmorphological characteristics of lettuce variety 45-100 RZ, a sample ofseed of said variety having been deposited under NCIMB accession No.42847, and other selected traits.

In particular, the invention relates to methods for producing a seed ofa 45-100 RZ-derived lettuce plant which may comprise (a) crossing aplant of lettuce variety 45-100 RZ, a sample of seed of which havingbeen deposited under NCIMB Accession No. NCIMB 42847, with a secondlettuce plant and (b) whereby seed of a 45-100 RZ-derived lettuce plantforms, wherein such a method may further comprise (c) crossing a plantgrown from 45-100 RZ-derived lettuce seed with itself or with a secondlettuce plant to yield additional 45-100 RZ-derived lettuce seed, (d)growing the additional 45-100 RZ-derived lettuce seed of step (c) toyield additional 45-100 RZ-derived lettuce plants and selecting plantsexhibitingone or more or all of the physiological and morphologicalcharacteristics of lettuce variety 45-100 RZ, and (e) repeating thecrossing and growing of steps (c) and (d) for an additional 3-10generations to further generate 45-100 RZ-derived lettuce plants thatexhibit one or more or all of the physiological and morphologicalcharacteristics of lettuce variety 45-100 RZ.

The invention additionally provides a method of introducing at least onenew trait into a plant of lettuce variety 45-100 RZ which may comprise:(a) crossing a plant of lettuce variety 45-100 RZ, a sample of seed ofwhich having been deposited under NCIMB Accession No. NCIMB 42847, witha second lettuce plant that may comprise at least one new trait toproduce progeny seed; (b) harvesting and planting the progeny seed toproduce at least one progeny plant of a subsequent generation, whereinthe progeny plant may comprise the at least one new trait; (c) crossingthe selected progeny plant with a plant of lettuce variety 45-100 RZ, toproduce backcross progeny seed; (d) harvesting and planting thebackcross progeny seed to produce a backcross progeny plant, (e)repeating steps (c) and (d) for at least three additional generations toproduce backcross progeny that may comprise the at least one new traitand all of the physiological and morphological characteristics of aplant of lettuce variety 45-100 RZ, when grown in the same environmentalconditions. The invention, of course, includes a lettuce plant producedby this method.

Backcrossing may also be used to improve an inbred plant. Backcrossingtransfers a specific desirable trait from one inbred or non-inbredsource to an inbred that lacks that trait. This may be accomplished, forexample, by first crossing a superior inbred (A) (recurrent parent) to adonor inbred (non-recurrent parent), which carries the appropriate locusor loci for the trait in question. The progeny of this cross are thenmated back to the superior recurrent parent (A) followed by selection inthe resultant progeny for the desired trait to be transferred from thenon-recurrent parent. After five or more backcross generations withselection for the desired trait, the progeny are heterozygous for locicontrolling the characteristic being transferred, but are like thesuperior parent for most or almost all other loci. The last backcrossgeneration would be selfed to give pure breeding progeny for the traitbeing transferred. When a plant of lettuce variety 45-100 RZ, a sampleof seed of which having been deposited under NCIMB Accession No. NCIMB42847, is used in backcrossing, offspring retaining one or more or allof the physiological and morphological characteristics of lettucevariety 45-100 RZ are progeny within the ambit of the invention.Backcrossing methods may be used with the present invention to improveor introduce a characteristic into a plant of the invention, being aplant of lettuce variety 45-100 RZ. See, e.g., U.S. Pat. No. 7,705,206(incorporated herein by reference consistent with the aboveINCORPORATION BY REFERENCE section), for a general discussion relatingto backcrossing.

The invention further involves a method of determining the genotype of aplant of lettuce variety 45-100 RZ, a sample of seed of which has beendeposited under NCIMB Accession No. NCIMB 42847, or a first generationprogeny thereof, which may comprise obtaining a sample of nucleic acidsfrom said plant and detecting in said nucleic acids a plurality ofpolymorphisms. This method may additionally comprise the step of storingthe results of detecting the plurality of polymorphisms on a computerreadable medium. The plurality of polymorphisms is indicative of and/orgive rise to the expression of the physiological and morphologicalcharacteristics of lettuce variety 45-100 RZ.

There are various ways of obtaining genotype data from a nucleic acidsample. Genotype data may be gathered which is specific for certainphenotypic traits (e.g. gene sequences), but also patterns of randomgenetic variation may be obtained to construct a so-called DNAfingerprint. Depending on the technique used a fingerprint may beobtained that is unique for lettuce variety 45-100 RZ. Obtaining aunique DNA fingerprint depends on the genetic variation present in avariety and the sensitivity of the fingerprinting technique. A techniqueknown in the art to provide a good fingerprint profile is called AFLPfingerprinting technique (See generally U.S. Pat. No. 5,874,215), butthere are many other marker based techniques, such as RFLP (orRestriction fragment length polymorphism), SSLP (or Simple sequencelength polymorphism), RAPD (or Random amplification of polymorphic DNA)VNTR (or Variable number tandem repeat), Microsatellite polymorphism,SSR (or Simple sequence repeat), STR (or Short tandem repeat), SFP (orSingle feature polymorphism) DArT (or Diversity Arrays Technology), RADmarkers (or Restriction site associated DNA markers) (e.g. Baird et al.PloS One Vol. 3 e3376, 2008; Semagn et al. African Journal ofBiotechnology Vol. 5 number 25 pp. 2540-2568, 29 Dec., 2006). Nowadays,sequence-based methods are utilizing Single Nucleotide Polymorphisms(SNPs) that are randomly distributed across genomes, as a common toolfor genotyping (e.g. Elshire et al. PloS One Vol. 6: e19379, 2011;Poland et al. PloS One Vol. 7: e32253; Truong et al. PLoS One Vol. 7number 5: e37565, 2012).

With any of the aforementioned genotyping techniques, polymorphisms maybe detected when the genotype and/or sequence of the plant of interestis compared to the genotype and/or sequence of one or more referenceplants. As used herein, the genotype and/or sequence of a referenceplant may be derived from, but is not limited to, any one of thefollowing: parental lines, closely related plant varieties or species,complete genome sequence of a related plant variety or species, or thede novo assembled genome sequence of one or more related plant varietiesor species. For example, it is possible to detect polymorphisms for thecharacteristic of head size by comparing the genotype and/or thesequence of lettuce variety 45-100 RZ with the genotype and/or thesequence of one or more reference plants. The reference plant(s) usedfor comparison in this example may for example be, but is not limitedto, the comparison variety Diurnas. It is also possible for example, todetect polymorphisms for head size by comparing the genotype and/or thesequence of lettuce variety 45-100 RZ with the genotype and/or thesequence of one or more reference plants. The reference plant(s) usedfor comparison may for example be, but is not limited to, the comparisonvariety Diurnas.

The polymorphism revealed by these techniques may be used to establishlinks between genotype and phenotype. The polymorphisms may thus be usedto predict or identify certain phenotypic characteristics, individuals,or even species. The polymorphisms are generally called markers. It iscommon practice for the skilled artisan to apply molecular DNAtechniques for generating polymorphisms and creating markers.

The polymorphisms of this invention may be provided in a variety ofmediums to facilitate use, e.g. a database or computer readable medium,which may also contain descriptive annotations in a form that allows askilled artisan to examine or query the polymorphisms and obtain usefulinformation.

As used herein “database” refers to any representation of retrievablecollected data including computer files such as text files, databasefiles, spreadsheet files and image files, printed tabulations andgraphical representations and combinations of digital and image datacollections. In a preferred aspect of the invention, “database” refersto a memory system that may store computer searchable information.

As used herein, “computer readable media” refers to any medium that maybe read and accessed directly by a computer. Such media include, but arenot limited to: magnetic storage media, such as floppy discs, hard disc,storage medium and magnetic tape; optical storage media such as CD-ROM;electrical storage media such as RAM, DRAM, SRAM, SDRAM, ROM; and PROMs(EPROM, EEPROM, Flash EPROM), and hybrids of these categories such asmagnetic/optical storage media. A skilled artisan may readily appreciatehow any of the presently known computer readable mediums may be used tocreate a manufacture which may comprise computer readable medium havingrecorded thereon a polymorphism of the present invention.

As used herein, “recorded” refers to the result of a process for storinginformation in a retrievable database or computer readable medium. Forinstance, a skilled artisan may readily adopt any of the presently knownmethods for recording information on computer readable medium togenerate media that may comprise the polymorphisms of the presentinvention. A variety of data storage structures are available to askilled artisan for creating a computer readable medium where the choiceof the data storage structure will generally be based on the meanschosen to access the stored information. In addition, a variety of dataprocessor programs and formats may be used to store the polymorphisms ofthe present invention on computer readable medium.

The present invention further provides systems, particularlycomputer-based systems, which contain the polymorphisms describedherein. Such systems are designed to identify the polymorphisms of thisinvention. As used herein, “a computer-based system” refers to thehardware, software and memory used to analyze the polymorphisms. Askilled artisan may readily appreciate that any one of the currentlyavailable computer-based system are suitable for use in the presentinvention.

Lettuce leaves are sold in packaged form, including without limitationas pre-packaged lettuce salad or as lettuce heads. Mention is made ofU.S. Pat. No. 5,523,136, incorporated herein by reference consistentwith the above INCORPORATION BY REFERENCE section, which providespackaging film, and packages from such packaging film, including suchpackaging containing leafy produce, and methods for making and usingsuch packaging film and packages, which are suitable for use with thelettuce leaves of the invention. Thus, the invention comprehends the useof and methods for making and using the leaves of the lettuce plant ofthe invention, as well as leaves of lettuce plants derived from theinvention. The invention further relates to a container which maycomprise one or more plants of the invention, or one or more lettuceplants derived from a plant of the invention, in a growth substrate forharvest of leaves from the plant in a domestic environment. This way theconsumer may pick very fresh leaves for use in salads. More generally,the invention includes one or more plants of the invention or one ormore plants derived from lettuce of the invention, wherein the plant isin a ready-to-harvest condition, including with the consumer picking hisown, and further including a container which may comprise one or more ofthese plants.

The invention is further described by the following numbered paragraphs:

1. A seed of lettuce variety 45-100 RZ, a sample of seed of said varietyhaving been deposited under NCIMB accession No. 42847.

2. A lettuce plant grown from the seed of paragraph 1.

3. The lettuce plant of paragraph 2, which is a plant grown from seedhaving been deposited under NCIMB accession No. 42847.

4. A lettuce plant, or a part thereof, having all the physiological andmorphological characteristics of the lettuce plant of paragraph 2.

5. A part of the plant of paragraph 2, wherein said part comprises amicrospore, pollen, ovary, ovule, embryo sac, egg cell, cutting, root,stem, cell or protoplast.

6. A tissue culture of regenerable cells or protoplasts from the lettuceplant of paragraph 2.

7. The tissue culture of paragraph 6, wherein said cells or protoplastsof the tissue culture are derived from a tissue comprising a leaf,pollen, embryo, cotyledon, hypocotyl, meristematic cell, root, root tip,anther, flower, seed or stem.

8. A lettuce plant regenerated from the tissue culture of paragraph 6,wherein the regenerated plant expresses all of the physiological andmorphological characteristics of lettuce variety 45-100 RZ, a sample ofseed of said variety having been deposited under NCIMB accession No.42847.

9. A method of vegetatively propagating a plant of lettuce variety45-100 RZ comprising (a) collecting tissue capable of being propagatedfrom a plant of lettuce 45-100 RZ, a sample of seed of said varietyhaving been deposited under NCIMB accession No. 42847, (b) cultivatingthe tissue to obtain proliferated shoots and rooting the proliferatedshoots to obtain rooted plantlets, and (c) optionally growing plantsfrom the rooted plantlets.

10. A method for producing a progeny plant of lettuce cultivar 45-100RZ, comprising crossing a plant designated 45-100 RZ with itself or withanother lettuce plant, harvesting the resultant seed, and growing saidseed.

11. A progeny plant produced by the method of paragraph 10, wherein saidprogeny plant exhibits a combination of traits including resistance tolettuce aphid Nasonovia ribisnigri (Mosley) biotype Nr:0, resistance toroot aphid (Pemphigus bursarius), resistance to downy mildew (Bremialactucae) races B1:1-33EU and Ca-I-VIII, mature medium to grey greenleaves with slight to no blistering and a medium size head.

12. A progeny plant produced by the method of paragraph 10, wherein saidprogeny exhibits all the morphological and physiological characteristicsof the lettuce variety designated 45-100 RZ, a sample of seed of saidvariety having been deposited under NCIMB accession No. 42847.

13. The progeny plant of paragraph 11, wherein said progeny plant ismodified in one or more other characteristics.

14. The progeny plant of paragraph 13, wherein the modification iseffected by mutagenesis.

15. The progeny plant of paragraph 13, wherein the modification iseffected by transformation with a transgene.

16. A method of producing a lettuce seed comprising crossing a maleparent lettuce plant with a female parent lettuce plant and harvestingthe resultant lettuce seed, wherein said male parent lettuce plant orsaid female parent lettuce plant is the lettuce plant of paragraph 2.

17. A lettuce seed produced by the method of paragraph 16.

18. A lettuce plant produced by growing the seed of paragraph 17.

19. A method for producing a seed of a 45-100 RZ-derived lettuce plantcomprising (a) crossing a plant of lettuce variety 45-100 RZ, a sampleof seed of which having been deposited under NCIMB Accession No. NCIMB42847, with a second lettuce plant, and (b) whereby seed of a 45-100RZ-derived lettuce plant forms.

20. The method of paragraph 19 further comprising (c) crossing a plantgrown from 45-100 RZ-derived lettuce seed with itself or with a secondlettuce plant to yield additional 45-100 RZ-derived lettuce seed, (d)growing the additional 45-100 RZ-derived lettuce seed of step (c) toyield additional 45-100 RZ-derived lettuce plants, and (e) repeating thecrossing and growing of steps (c) and (d) for an additional 3-10generations to generate further 45-100 RZ-derived lettuce plants, and(f) whereby seed of a 45-100 RZ-derived lettuce plant forms.

21. A seed produced by the method of paragraph 19.

22. A plant grown from the seed produced by the method of paragraph 21.

23. A method of introducing at least one new trait into a plant oflettuce variety 45-100 RZ comprising: (a) crossing a plant of lettucevariety 45-100 RZ, a sample of seed of which having been deposited underNCIMB Accession No. NCIMB 42847, with a second lettuce plant thatcomprises at least one new trait to produce progeny seed, (b) harvestingand planting the progeny seed to produce at least one progeny plant of asubsequent generation, wherein the progeny plant comprises the at leastone new trait, (c) crossing the progeny plant with a plant of lettucevariety 45-100 RZ to produce backcross progeny seed, (d) harvesting andplanting the backcross progeny seed to produce a backcross progenyplant, and (e) repeating steps (c) and (d) for at least three additionalgenerations to produce a lettuce plant of variety 45-100 RZ comprisingat least one new trait and all of the physiological and morphologicalcharacteristics of a plant of lettuce variety 45-100 RZ, when grown inthe same environmental conditions.

24. A method of producing a plant of lettuce variety 45-100 RZcomprising at least one new trait, the method comprising introducing amutation or transgene conferring the at least one new trait into a plantof lettuce variety 45-100 RZ, wherein a sample of seed of said varietyhas been deposited under NCIMB Accession No. NCIMB 42847.

25. The lettuce plant produced by the method of paragraph 23.

26. A method for producing lettuce leaves as a food product comprisingsowing the seed of a paragraph 1 and growing the seed into a harvestablelettuce plant and harvesting the head or leaves of said plant.

27. A method for producing lettuce leaves as a fresh vegetablecomprising packaging leaves of a plant of paragraph 2.

28. A method for producing lettuce leaves as a processed food comprisingprocessing leaves of a plant of paragraph 2.

29. A container comprising one or more lettuce plants of paragraph 2 forharvest of leaves.

30. A method of determining the genotype of a plant of lettuce variety45-100 RZ, a sample of seed of which has been deposited under NCIMBAccession No. NCIMB 42847, or a first generation progeny thereof,comprising obtaining a sample of nucleic acids from said plant andcomparing said nucleic acids to a sample of nucleic acids obtained froma reference plant, and detecting a plurality of polymorphisms betweenthe two nucleic acid samples, wherein the plurality of polymorphisms areindicative of lettuce variety 45-100 RZ and/or give rise to theexpression of any one or more, or all, of the physiological andmorphological characteristics of lettuce variety 45-100 RZ of paragraph2.

31. A lettuce plant produced by the method of paragraph 24.

Having thus described in detail preferred embodiments of the presentinvention, it is to be understood that the invention is not to belimited to particular details set forth in the above description as manyapparent variations thereof are possible without departing from thespirit or scope of the present invention.

What is claimed is:
 1. A seed of lettuce variety 45-100 RZ, a sample ofseed of said variety having been deposited under NCIMB accession No.42847.
 2. A lettuce plant grown from the seed of claim
 1. 3. The lettuceplant of claim 2, which is a plant grown from seed having been depositedunder NCIMB accession No.
 42847. 4. A lettuce plant, or a part thereof,having all the physiological and morphological characteristics of thelettuce plant of claim
 2. 5. A part of the plant of claim 2, whereinsaid part comprises a microspore, pollen, ovary, ovule, embryo sac, eggcell, cutting, root, stem, cell or protoplast.
 6. A tissue culture ofregenerable cells or protoplasts from the lettuce plant of claim
 2. 7.The tissue culture as claimed in claim 6, wherein said cells orprotoplasts of the tissue culture are derived from a tissue comprising aleaf, pollen, embryo, cotyledon, hypocotyl, meristematic cell, root,root tip, anther, flower, seed or stem.
 8. A lettuce plant regeneratedfrom the tissue culture of claim 6, wherein the regenerated plantexpresses all of the physiological and morphological characteristics oflettuce variety 45-100 RZ, a sample of seed of said variety having beendeposited under NCIMB accession No.
 42847. 9. A method of vegetativelypropagating a plant of lettuce variety 45-100 RZ comprising (a)collecting tissue capable of being propagated from a plant of lettuce45-100 RZ, a sample of seed of said variety having been deposited underNCIMB accession No. 42847, (b) cultivating the tissue to obtainproliferated shoots and rooting the proliferated shoots to obtain rootedplantlets, and (c) optionally growing plants from the rooted plantlets.10. A method for producing a progeny plant of lettuce cultivar 45-100RZ, comprising crossing a plant designated 45-100 RZ with itself or withanother lettuce plant, harvesting the resultant seed, and growing saidseed.
 11. A progeny plant produced by the method of claim 10, whereinsaid progeny plant exhibits a combination of traits including resistanceto lettuce aphid Nasonovia ribisnigri (Mosley) biotype Nr:0, resistanceto root aphid (Pemphigus bursarius), resistance to downy mildew (Bremialactucae) races B1:1-33EU and Ca-I-VIII, mature medium to grey greenleaves with slight to no blistering and a medium size head.
 12. Aprogeny plant produced by the method of claim 10, wherein said progenyexhibits all the morphological and physiological characteristics of thelettuce variety designated 45-100 RZ, a sample of seed of said varietyhaving been deposited under NCIMB accession No.
 42847. 13. The progenyplant as claimed in claim 11, wherein said progeny plant is modified inone or more other characteristics.
 14. The progeny plant as claimed inclaim 13, wherein the modification is effected by mutagenesis.
 15. Theprogeny plant as claimed in claim 13, wherein the modification iseffected by transformation with a transgene.
 16. A method of producing alettuce seed comprising crossing a male parent lettuce plant with afemale parent lettuce plant and harvesting the resultant lettuce seed,wherein said male parent lettuce plant or said female parent lettuceplant is the lettuce plant of claim
 2. 17. A lettuce seed produced bythe method of claim
 16. 18. A lettuce plant produced by growing the seedof claim
 17. 19. A method for producing a seed of a 45-100 RZ-derivedlettuce plant comprising (a) crossing a plant of lettuce variety 45-100RZ, a sample of seed of which having been deposited under NCIMBAccession No. NCIMB 42847, with a second lettuce plant, and (b) wherebyseed of a 45-100 RZ-derived lettuce plant forms.
 20. The method of claim19 further comprising (c) crossing a plant grown from 45-100 RZ-derivedlettuce seed with itself or with a second lettuce plant to yieldadditional 45-100 RZ-derived lettuce seed, (d) growing the additional45-100 RZ-derived lettuce seed of step (c) to yield additional 45-100RZ-derived lettuce plants, and (e) repeating the crossing and growing ofsteps (c) and (d) for an additional 3-10 generations to generate further45-100 RZ-derived lettuce plants, and (f) whereby seed of a 45-100RZ-derived lettuce plant forms.
 21. A seed produced by the method ofclaim
 19. 22. A plant grown from the seed of claim
 21. 23. A method ofintroducing at least one new trait into a plant of lettuce variety45-100 RZ comprising: (a) crossing a plant of lettuce variety 45-100 RZ,a sample of seed of which having been deposited under NCIMB AccessionNo. NCIMB 42847, with a second lettuce plant that comprises at least onenew trait to produce progeny seed, (b) harvesting and planting theprogeny seed to produce at least one progeny plant of a subsequentgeneration, wherein the progeny plant comprises the at least one newtrait, (c) crossing the progeny plant with a plant of lettuce variety45-100 RZ to produce backcross progeny seed, (d) harvesting and plantingthe backcross progeny seed to produce a backcross progeny plant, and (e)repeating steps (c) and (d) for at least three additional generations toproduce a lettuce plant of variety 45-100 RZ comprising at least one newtrait and all of the physiological and morphological characteristics ofa plant of lettuce variety 45-100 RZ, when grown in the sameenvironmental conditions.
 24. A method of producing a plant of lettucevariety 45-100 RZ comprising at least one new trait, the methodcomprising introducing a mutation or transgene conferring the at leastone new trait into a plant of lettuce variety 45-100 RZ, wherein asample of seed of said variety has been deposited under NCIMB AccessionNo. NCIMB
 42847. 25. The lettuce plant produced by the method of claim23.
 26. A method for producing lettuce leaves as a food productcomprising sowing the seed of a claim 1 and growing the seed into aharvestable lettuce plant and harvesting the head or leaves of saidplant.
 27. A method for producing lettuce leaves as a fresh vegetablecomprising packaging leaves of a plant of claim
 2. 28. A method forproducing lettuce leaves as a processed food comprising processingleaves of a plant of claim
 2. 29. A container comprising one or morelettuce plants of claim 2 for harvest of leaves.
 30. A method ofdetermining the genotype of a plant of lettuce variety 45-100 RZ, asample of seed of which has been deposited under NCIMB Accession No.NCIMB 42847, or a first generation progeny thereof, comprising obtaininga sample of nucleic acids from said plant and comparing said nucleicacids to a sample of nucleic acids obtained from a reference plant, anddetecting a plurality of polymorphisms between the two nucleic acidsamples, wherein the plurality of polymorphisms are indicative oflettuce variety 45-100 RZ and/or give rise to the expression of any oneor more, or all, of the physiological and morphological characteristicsof lettuce variety 45-100 RZ as claimed in claim
 2. 31. A lettuce plantproduced by the method of claim 24.